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Ab120560

Manufactured by Abcam
Sourced in United Kingdom, United States

Ab120560 is an antibody-based product for research use. It serves as a tool for detecting and quantifying a specific target protein. The product details and performance characteristics are available for review.

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4 protocols using ab120560

1

Investigating MAPK Signaling in Virus Infection

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Anti-phospho-p38 MAPK (Thr180/Tyr182) (9211S, Cell Signaling Technology), anti-p38α (sc-535, Santa Cruz), anti-Lamin B1(66095-1-Ig, Proteintech), anti-phospho-ERK(sc-81492, Santa Cruz), anti-phospho-JNK(sc-6254, Santa Cruz), anti-GAPDH (M20006; Abmart), anti-gag (ab63917, Abcam), anti-p24 (mouse ascites antibody), Alexa Fluor® 488 AffiniPure Goat Anti-Mouse IgG (Jackson Immunoresearch), Rhodamine(TRITC) AffiniPure Goat Anti-Rabbit IgG (Jackson Immunoresearch). α7 nicotinic acetylcholine receptor agonist: GTS-21 (ab120560, Abcam), DUSP1 and DUSP6 inhibitor: BCI (T10486, Topscience), ROS scavenger: N-Acetyl-L-methionine (T8059, Topscience).
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2

Electro-Acupuncture and GTS21 in Sepsis

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After CLP operation, a two-day EA treatment or GTS21 administration was performed once a day. For EA treatment, after determining the localization of certain acupoints (Zusanli-ST36, Quchi-LI11, and Tianshu-ST25), rats were acupunctured with a 0.35 mm diameter needle without any hand-technique like lifting, thrusting, and rotating. Then, a stimulation at an intensity of 2 V (load voltage) and a frequency of 3 Hz was given for 15 minutes using the Electronic Acupuncture Treatment Instrument (96805- I Type, Xinsheng Industrial Limited Liability Company, Qingdao, China). For GTS21 (a specific agonist of α7nAchR; ab120560, Abcam, England) administration, liquid medicine was injected to CLP rats intraperitoneally with a dose of 4 mg/kg/d for two days [28 (link)].
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3

Neurochemical and Behavioral Effects of Drug Cocktail

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Varenicline tartate (1.5 mg/kg, Toronto Research Chemicals, V098490), nicotine hydrogen tartate (0.1, 0.5, and 1.5 mg/kg, Glentham Life Sciences, GL9693), and morphine (10 mg/kg, Sigma-Aldrich, M8777) were dissolved in saline. GTS 21 (4 mg/kg, Abcam, ab120560), a partial agonist of the α7 nAChR, was dissolved in DMSO. Stock solutions were aliquoted and frozen. Prior to experiments, stock solutions were diluted with saline to the appropriate concentrations for injection. 200 proof ethanol (2 g/kg) was diluted 1:4 in saline. Mice received injections of 100 μL solution per 10 g of body weight. A varenicline dose that was previously shown to increase NAc DA and attenuate nicotine-evoked NAc DA in vivo in rodents was chosen (Ericson et al., 2009 (link)). Varenicline also decreases ethanol consumption at the dose selected (Steensland et al., 2007 ). Drug doses that we have shown to significantly elevate GRAB-DA signal in the NAc were used (Alhadeff et al., 2019 ). Nicotine doses for feeding experiments were selected based on prior work showing nicotine’s long-term anorexic effects in mice (Mineur et al., 2011 (link)).
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4

Modulation of Th1/Th2 Differentiation

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CD4+ T cells were incubated in the presence of anti-CD3/CD28 alone or with CSE, IL-12 (20 ng/mL), IL-4 (20 ng/mL) or GTS-21 (#ab120560, an agonist for the α7 nAChR; Abcam; Cambridge, USA, 10 μmol/l), and then α7 nAChR expression and Th1/Th2 differentiation were evaluated.
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